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Ondansetron

NDC 51407-004 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGolden State Medical Supply, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077851
Dosage form / routeTABLET · ORAL
Active ingredientsONDANSETRON HYDROCHLORIDE (8 mg/1)
Marketing started20070625
Package count2

External sources

Source: openFDA. Public-domain (CC0).